Exposure to specific environments that have been associated with past alcohol use is thought to contribute to propensity to relapse in human alcoholics. We employ an animal model for relapse triggered by ethanol-associated environments. In this model, subjects acquire an ethanol self-administration habit in a distinctive context, and then undergo a period of extinction in a second distinctive context during which ethanol is no longer available and ethanol seeking by the subjects diminishes. However, when the subjects are placed once again into the ethanol-associated context, ethanol-seeking is robustly renewed, indicating that the context has acquired the ability to motivate responding due to its predictive relationship with ethanol self-administration. The studies within this proposal will begin to define the underlying neural circuit for this context-dependent reinstatement. Studies in the first aim will test whether context-dependent reinstatement for ethanol seeking depends upon DAergic transmission. Studies within the second aim will use reversible inactivation to determine whether the expression of context-dependent reinstatement for ethanol depends upon the hippocampus (HIPP), and will further define the importance of the hippocampal projection to the nucleus accumbens (NAC) in the behavior, by reversibly inactivating the two brain regions in opposite hemispheres (a disconnection). Next in vivo electrophysiology in awake rats will be used to test the hypothesis that neural activity within the NAC and HIPP is context-specific by comparing responses of individual neurons when subjects are exposed to the context previously associated with ethanol, and to the extinction context in which instrumental responding was not reinforced by ethanol. Hence this aim will test whether distinct contextual representations exist in either one or both of these two regions, defining a possible neurophysiological basis for context-dependent reinstatement. Taken together this set of studies will begin to define the neurochemical, neuroanatomical, and neurophysiological basis for context-dependent reinstatement of ethanol seeking. These results will provide new understanding of the possible biological mechanisms that underlie context-dependent relapse in humans, and may lead to new treatment strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA014925-02
Application #
6884891
Study Section
Neurotoxicology and Alcohol Study Section (NAL)
Program Officer
Egli, Mark
Project Start
2004-05-01
Project End
2009-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
2
Fiscal Year
2005
Total Cost
$362,475
Indirect Cost
Name
Ernest Gallo Clinic and Research Center
Department
Type
DUNS #
173995366
City
Emeryville
State
CA
Country
United States
Zip Code
94608
Millan, E Zayra; Kim, H Amy; Janak, Patricia H (2017) Optogenetic activation of amygdala projections to nucleus accumbens can arrest conditioned and unconditioned alcohol consummatory behavior. Neuroscience 360:106-117
Richard, Jocelyn M; Ambroggi, Frederic; Janak, Patricia H et al. (2016) Ventral Pallidum Neurons Encode Incentive Value and Promote Cue-Elicited Instrumental Actions. Neuron 90:1165-1173
Corbit, Laura H; Janak, Patricia H (2016) Habitual Alcohol Seeking: Neural Bases and Possible Relations to Alcohol Use Disorders. Alcohol Clin Exp Res 40:1380-9
Corbit, Laura H; Fischbach, Sarah C; Janak, Patricia H (2016) Nucleus accumbens core and shell are differentially involved in general and outcome-specific forms of Pavlovian-instrumental transfer with alcohol and sucrose rewards. Eur J Neurosci 43:1229-36
Corbit, Laura H; Janak, Patricia H (2016) Changes in the Influence of Alcohol-Paired Stimuli on Alcohol Seeking across Extended Training. Front Psychiatry 7:169
Keiflin, Ronald; Janak, Patricia H (2015) Dopamine Prediction Errors in Reward Learning and Addiction: From Theory to Neural Circuitry. Neuron 88:247-63
Millan, E Zayra; Reese, Rebecca M; Grossman, Cooper D et al. (2015) Nucleus Accumbens and Posterior Amygdala Mediate Cue-Triggered Alcohol Seeking and Suppress Behavior During the Omission of Alcohol-Predictive Cues. Neuropsychopharmacology 40:2555-65
Sangha, Susan (2015) Plasticity of Fear and Safety Neurons of the Amygdala in Response to Fear Extinction. Front Behav Neurosci 9:354
Sciascia, Joanna M; Reese, Rebecca M; Janak, Patricia H et al. (2015) Alcohol-Seeking Triggered by Discrete Pavlovian Cues is Invigorated by Alcohol Contexts and Mediated by Glutamate Signaling in the Basolateral Amygdala. Neuropsychopharmacology 40:2801-12
Janak, Patricia H; Tye, Kay M (2015) From circuits to behaviour in the amygdala. Nature 517:284-92

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